GB823180A - Improvements in the production of epoxidic compounds - Google Patents

Improvements in the production of epoxidic compounds

Info

Publication number
GB823180A
GB823180A GB35480/57A GB3548057A GB823180A GB 823180 A GB823180 A GB 823180A GB 35480/57 A GB35480/57 A GB 35480/57A GB 3548057 A GB3548057 A GB 3548057A GB 823180 A GB823180 A GB 823180A
Authority
GB
United Kingdom
Prior art keywords
acid
esters
methyl
unsaturated
alcohols
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB35480/57A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Huels AG
Original Assignee
Chemische Werke Huels AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chemische Werke Huels AG filed Critical Chemische Werke Huels AG
Publication of GB823180A publication Critical patent/GB823180A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/18Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/20Ethers with hydroxy compounds containing no oxirane rings
    • C07D303/22Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/16Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by esterified hydroxyl radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Epoxidic compounds are produced by treating with peracetic acid an ester or ether of an unsaturated alcohol of the general formula <FORM:0823180/IV (a)/1> in which R represents hydrogen or an alkyl radical and R1 an alkyl radical. Suitable alcohols for the formation of the ether and ester starting materials are those in which R represents hydrogen or methyl, and R1 is methyl, ethyl or propyl. They may be obtained by dehydration of the corresponding 1.3-diols or by partial hydrogenation of unsaturated 2-alkyl branched aldehyde. By pyrolysis of the diacetates which are formed by acetylation of the 2-alkyl branched 1,3-diols (readily accessible by aldol condensation and subsequent hydrogenation) there are obtained the mono-acetates of unsaturated 2-alkyl branched alcohols of the above formula. These acetates may be readily re-esterified especially with methyl esters. After saponification, they may be esterified with monobasic or polybasic acids or acid anhydrides, for example acetic acid, adipic acid, phthalic acid, epoxytetrahydrophthalic acid, phosphoric acid, mono- or di-alkylphosphoric acid or sulphonic acids to esters, or reacted with alcohols, glycols, polyglycols, thioglycols, diethanolamine or diphenylolpropane to ethers. These ethers and esters are then epoxidized by dripping into peracetic acid in glacial acetic acid or acetone at 30 DEG to 35 DEG C. and then stirring for 5 to 6 hours at the same temperature.
GB35480/57A 1957-04-10 1957-11-14 Improvements in the production of epoxidic compounds Expired GB823180A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE823180X 1957-04-10

Publications (1)

Publication Number Publication Date
GB823180A true GB823180A (en) 1959-11-04

Family

ID=6745510

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35480/57A Expired GB823180A (en) 1957-04-10 1957-11-14 Improvements in the production of epoxidic compounds

Country Status (1)

Country Link
GB (1) GB823180A (en)

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